Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 7 |
GO:0042995 | cell projection | 2 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 7 |
Related structures:
AlphaFold database: E9AQN1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 11 | 15 | PF00656 | 0.518 |
CLV_C14_Caspase3-7 | 80 | 84 | PF00656 | 0.495 |
CLV_C14_Caspase3-7 | 88 | 92 | PF00656 | 0.487 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 505 | 507 | PF00675 | 0.632 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 505 | 507 | PF00082 | 0.632 |
CLV_PCSK_PC1ET2_1 | 111 | 113 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 451 | 455 | PF00082 | 0.531 |
DEG_APCC_DBOX_1 | 458 | 466 | PF00400 | 0.546 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.572 |
DEG_SPOP_SBC_1 | 168 | 172 | PF00917 | 0.411 |
DOC_CKS1_1 | 197 | 202 | PF01111 | 0.454 |
DOC_CKS1_1 | 476 | 481 | PF01111 | 0.494 |
DOC_CYCLIN_RxL_1 | 214 | 222 | PF00134 | 0.422 |
DOC_CYCLIN_yClb3_PxF_3 | 204 | 210 | PF00134 | 0.423 |
DOC_CYCLIN_yCln2_LP_2 | 197 | 203 | PF00134 | 0.452 |
DOC_MAPK_RevD_3 | 264 | 279 | PF00069 | 0.435 |
DOC_PP2B_LxvP_1 | 126 | 129 | PF13499 | 0.402 |
DOC_PP2B_LxvP_1 | 202 | 205 | PF13499 | 0.563 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.308 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.552 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.696 |
LIG_14-3-3_CanoR_1 | 166 | 175 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 30 | 36 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 315 | 322 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 363 | 370 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 457 | 463 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 505 | 515 | PF00244 | 0.651 |
LIG_Actin_WH2_2 | 137 | 154 | PF00022 | 0.384 |
LIG_BIR_III_2 | 485 | 489 | PF00653 | 0.552 |
LIG_BRCT_BRCA1_1 | 119 | 123 | PF00533 | 0.462 |
LIG_BRCT_BRCA1_1 | 524 | 528 | PF00533 | 0.385 |
LIG_Clathr_ClatBox_1 | 335 | 339 | PF01394 | 0.248 |
LIG_CSL_BTD_1 | 126 | 129 | PF09270 | 0.402 |
LIG_eIF4E_1 | 396 | 402 | PF01652 | 0.403 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.436 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.662 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.331 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.417 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.552 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.611 |
LIG_FHA_2 | 398 | 404 | PF00498 | 0.540 |
LIG_FHA_2 | 506 | 512 | PF00498 | 0.615 |
LIG_FHA_2 | 78 | 84 | PF00498 | 0.516 |
LIG_LIR_Nem_3 | 120 | 126 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 34 | 39 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 388 | 392 | PF02991 | 0.311 |
LIG_MYND_1 | 200 | 204 | PF01753 | 0.459 |
LIG_PDZ_Class_2 | 525 | 530 | PF00595 | 0.405 |
LIG_Pex14_1 | 32 | 36 | PF04695 | 0.539 |
LIG_Pex14_2 | 123 | 127 | PF04695 | 0.459 |
LIG_SH2_GRB2like | 396 | 399 | PF00017 | 0.366 |
LIG_SH2_NCK_1 | 370 | 374 | PF00017 | 0.631 |
LIG_SH2_SRC | 418 | 421 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.415 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.613 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.505 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.443 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.410 |
LIG_SH3_3 | 473 | 479 | PF00018 | 0.476 |
LIG_SUMO_SIM_anti_2 | 271 | 276 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 217 | 222 | PF11976 | 0.358 |
LIG_TRAF2_1 | 41 | 44 | PF00917 | 0.587 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.497 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.686 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.488 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.697 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.760 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.636 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.450 |
MOD_CK2_1 | 505 | 511 | PF00069 | 0.527 |
MOD_GlcNHglycan | 220 | 224 | PF01048 | 0.537 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.569 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.655 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.553 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.626 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.586 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.674 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.712 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.368 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.404 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.298 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.377 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.540 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.394 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.548 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.503 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.619 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.626 |
MOD_N-GLC_1 | 245 | 250 | PF02516 | 0.440 |
MOD_N-GLC_1 | 397 | 402 | PF02516 | 0.408 |
MOD_N-GLC_1 | 470 | 475 | PF02516 | 0.620 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.298 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.343 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.335 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.528 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.307 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.398 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.566 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.578 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.370 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.559 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.518 |
MOD_NEK2_2 | 133 | 138 | PF00069 | 0.384 |
MOD_NEK2_2 | 169 | 174 | PF00069 | 0.387 |
MOD_NEK2_2 | 212 | 217 | PF00069 | 0.410 |
MOD_NEK2_2 | 31 | 36 | PF00069 | 0.492 |
MOD_NEK2_2 | 446 | 451 | PF00069 | 0.579 |
MOD_PIKK_1 | 492 | 498 | PF00454 | 0.634 |
MOD_PKA_1 | 505 | 511 | PF00069 | 0.610 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.345 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.597 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.534 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.546 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.658 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.565 |
MOD_PKB_1 | 65 | 73 | PF00069 | 0.562 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.505 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.374 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.397 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.546 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.409 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.450 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.563 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.483 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.756 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.695 |
MOD_SUMO_rev_2 | 417 | 423 | PF00179 | 0.409 |
TRG_DiLeu_BaEn_1 | 511 | 516 | PF01217 | 0.499 |
TRG_DiLeu_BaLyEn_6 | 197 | 202 | PF01217 | 0.472 |
TRG_DiLeu_BaLyEn_6 | 214 | 219 | PF01217 | 0.459 |
TRG_DiLeu_BaLyEn_6 | 331 | 336 | PF01217 | 0.280 |
TRG_ER_diArg_1 | 277 | 279 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 505 | 507 | PF00400 | 0.632 |
TRG_NES_CRM1_1 | 413 | 427 | PF08389 | 0.304 |
TRG_NES_CRM1_1 | 46 | 57 | PF08389 | 0.387 |
TRG_Pf-PMV_PEXEL_1 | 112 | 116 | PF00026 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 162 | 167 | PF00026 | 0.312 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJG7 | Leptomonas seymouri | 36% | 100% |
A0A3S5H6X5 | Leishmania donovani | 84% | 100% |
A4H8J4 | Leishmania braziliensis | 68% | 100% |
A4HWW9 | Leishmania infantum | 85% | 100% |
Q4QEU7 | Leishmania major | 83% | 100% |